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	341.	4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate. [electronic resource] by Kobayashi, J Kimijima, Y Yamada, S Amagasa, T Saito-Ohara, F Producer: 20001012 In: Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	Extensive cytogenetic analysis of a stable dicentric isochromosome 21, idic(21), formed by fusion of the terminal long arms. [electronic resource] by Wandall, A Andersen, C Østergaard, M Koch, Jørn Producer: 20030109 In: Cytogenetic and genome research vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	343.	Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening. [electronic resource] by Graf, Michael D Gill, Prabhcharan Krew, Michael Schwartz, Stuart Producer: 20030213 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	344.	Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparations. [electronic resource] by Sanz, R Lorda-Sanchez, I Fernández-Moya, J M Cifuentes-Sulzberger, S Rodríguez de Alba, M Gonzalez-Gonzalez, M C Ibañez, M A Robledo, M Ayuso, C Ramos, C Producer: 20010419 In: Fetal diagnosis and therapy vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Acute myeloid leukaemia with +i(12p) shortly after treatment of mediastinal germ cell tumour. [electronic resource] by Vlasveld, L T Splinter, T A Hagemeijer, A Van Lom, K Löwenberg, B Producer: 19950130 In: British journal of haematology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	346.	FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2). [electronic resource] by Schaad, K Strömbeck, B Mandahl, N Andersen, M K Heim, S Mertens, F Johansson, B Producer: 20060728 In: Cytogenetic and genome research vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	347.	The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markers. [electronic resource] by Meggendorfer, M Haferlach, C Zenger, M Macijewski, K Kern, W Haferlach, T Producer: 20180212 In: Leukemia vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	348.	Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p. [electronic resource] by Wu, Yi-Cheng Fang, Jye Siung Lee, Kuei-Fang Estipona, Judy Yang, Man-Li Yuan, Chiou-Chung Producer: 20030812 In: Prenatal diagnosis vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	349.	Incidence of TCR and TCL1 gene translocations and isochromosome 7q in peripheral T-cell lymphomas using fluorescence in situ hybridization. [electronic resource] by Feldman, Andrew L Law, Mark Grogg, Karen L Thorland, Erik C Fink, Stephanie Kurtin, Paul J Macon, William R Remstein, Ellen D Dogan, Ahmet Producer: 20080822 In: American journal of clinical pathology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	350.	aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy. [electronic resource] by Theisen, Aaron Rosenfeld, Jill A Farrell, Sandra A Harris, Catharine J Wetzel, Heather H Torchia, Beth A Bejjani, Bassem A Ballif, Blake C Shaffer, Lisa G Producer: 20090618 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders. [electronic resource] by Herry, Angèle Douet-Guilbert, Nathalie Morel, Frédéric Le Bris, Marie-Josée Guéganic, Nadia Berthou, Christian De Braekeleer, Marc Producer: 20100730 In: Cancer genetics and cytogenetics vol. 200 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	352.	Consistency of isochromosome 7q and trisomy 8 in hepatosplenic gammadelta T-cell lymphoma: detection by fluorescence In situ hybridization of a splenic touch-preparation from a pediatric patient. [electronic resource] by Coventry, S Punnett, H H Tomczak, E Z Casher, D Koehler, M Borowitz, M J Griffin, C A de Chadarévian, J P Producer: 19990902 In: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	353.	Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. [electronic resource] by Leichtman, L G Zackowski, J L Storto, P D Newlin, A Producer: 19961209 In: American journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	354.	Fluorescence in situ hybridization analysis of chromosome 12 anomalies in semen cells from patients with carcinoma in situ of the testis. [electronic resource] by Meng, F J Zhou, Y Giwercman, A Skakkebaek, N E Geurts van Kessel, A D Suijkerbuijk, R F Producer: 19990426 In: The Journal of pathology vol. 186 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	355.	Concomitant appearance of trisomy 8 and isochromosome 17q in a Philadelphia-positive clone in a patient with chronic myeloid leukemia in chronic phase: an alarm for changing therapeutic strategy. [electronic resource] by Orciuolo, Enrico Buda, Gabriele Galimberti, Sara Sordi, Elisabetta Cervetti, Giulia Petrini, Mario Producer: 20071023 In: Cancer genetics and cytogenetics vol. 177 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	356.	The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements. [electronic resource] by McGowan, Kathryn D Weiser, Joseph J Horwitz, Juli Berend, Sue Ann McCaskill, Christopher Sutton, V Reid Shaffer, Lisa G Producer: 20020412 In: Prenatal diagnosis vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	357.	Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature. [electronic resource] by Manola, Kalliopi N Karakosta, Maria Sambani, Constantina Terzoudi, Georgia Pagoni, Maria Gatsa, Eleni Papaioannou, Maria Producer: 20100419 In: Acta haematologica vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	358.	Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype. [electronic resource] by Wang, Jia-Chi Vaccarello-Cruz, Mary Ross, Leslie Owen, Renius Pratt, Victoria M Lightman, Katherine Liu, Yan Hafezi, Katayoun Cherif, Dhia Sahoo, Trilochan Producer: 20140214 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	359.	Cytogenetic and molecular characterization of two isodicentric Y chromosomes. [electronic resource] by Stankiewicz, P Hélias-Rodzewicz, Z Jakubów-Durska, K Bocian, E Obersztyn, E Rappold, G A Mazurczak, T Producer: 20010712 In: American journal of medical genetics vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype. [electronic resource] by Goumy, C Beaufrère, A M Francannet, C Tchirkov, A Laurichesse Delmas, H Geissler, F Lemery, D Dechelotte, P J Vago, P Producer: 20060629 In: Prenatal diagnosis vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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